Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.
Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Unique Features of Germline Variation in Five Egyptian Familial Breast Cancer Families Revealed by Exome Sequencing.
Plos One
Kim, Yeong C YC; Soliman, Amr S AS; Cui, Jian J; Ramadan, Mohamed M; Hablas, Ahmed A; Abouelhoda, Mohamed M; Hussien, Nehal N; Ahmed, Ola O; Zekri, Abdel-Rahman Nabawy AN; Seifeldin, Ibrahim A IA; Wang, San Ming SM
LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome.
Journal Of Medical Genetics
Volikos, E E; Robinson, J J; Aittomäki, K K; Mecklin, J-P JP; Järvinen, H H; Westerman, A M AM; de Rooji, F W M FW; Vogel, T T; Moeslein, G G; Launonen, V V; Tomlinson, I P M IP; Silver, A R J AR; Aaltonen, L A LA